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US - Sr. Clinical Research Associate
∑ Assists with, attends, and may present at Investigator Meetings for assigned studies.
∑ Performs study close-out visits.
∑ Serves as mentor for more junior CRAs as well as new CRAs to the project.
∑ May conduct field training and assessment of CRA Is and CRA IIs.
∑ Authorized to request site audits for reasons of validity.
∑ Performs other duties as requested.
∑ Strong knowledge of clinical research process and medical terminology.
∑ At least four years experience in monitoring clinical trials preferred.
∑ Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
∑ Excellent organizational and interpersonal skills.
∑ Ability to interact with all levels of staff to coordinate/execute study activities.
∑ Ability to handle several priorities within multiple, complex clinical trials.
∑ Ability to reason independently and recommend specific solutions in clinical settings.
∑ Able to mentor other CRAs on project team and co-monitor as required.
∑ Understanding of basic data processing functions, including electronic data capture.
∑ Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research.
∑ Able to qualify for a major credit card.
∑ Valid driverís license; ability to rent automobile.
∑ Willingness and ability to travel domestically and internationally, as required.
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